Regulation of α2B-Adrenergic Receptor Cell Surface Transport by GGA1 and GGA2

• Published in: Scientific reports 2016-11, Vol.6 (1), p.37921-37921, Article 37921
• Main Authors: Zhang, Maoxiang, Huang, Wei, Gao, Jie, Terry, Alvin V., Wu, Guangyu
• Format: Article
• Language: English
• Subjects: 14/35; 14/63; 38/89; 631/80/313; 692/4017; 82; 82/29; 82/83; 96/109; 96/31; 96/95; Humanities and Social Sciences; multidisciplinary; Science
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep37921

The molecular mechanisms that control the targeting of newly synthesized G protein-coupled receptors (GPCRs) to the functional destinations remain poorly elucidated. Here, we have determined the role of Golgi-localized, γ-adaptin ear domain homology, ADP ribosylation factor-binding proteins 1 and 2 (GGA1 and GGA2) in the cell surface transport of α 2B -adrenergic receptor (α 2B -AR), a prototypic GPCR, and studied the underlying mechanisms. We demonstrated that knockdown of GGA1 and GGA2 by shRNA and siRNA significantly reduced the cell surface expression of inducibly expressed α 2B -AR and arrested the receptor in the perinuclear region. Knockdown of each GGA markedly inhibited the dendritic expression of α 2B -AR in primary cortical neurons. Consistently, depleting GGA1 and GGA2 attenuated receptor-mediated signal transduction measured as ERK1/2 activation and cAMP inhibition. Although full length α 2B -AR associated with GGA2 but not GGA1, its third intracellular loop was found to directly interact with both GGA1 and GGA2. More interestingly, further mapping of interaction domains showed that the GGA1 hinge region and the GGA2 GAE domain bound to multiple subdomains of the loop. These studies have identified an important function and revealed novel mechanisms of the GGA family proteins in the forward trafficking of a cell surface GPCR.